Technology and Software

Eurotherm Data Reviewer is a software application designed for the viewing, analysis and printing of historical data files obtained from Eurotherm data acquisition equipment.

Find and analyze data quickly, including by instrument group or batch.

The Audi...

A compact 1/4 DIN recorder with precision PID control option. 

• Digital batch recording and electronic signatures aid compliance to FDA 21 CFR Part 11 regulation and Data Integrity ALCOA+ principles • Can reduce capex using preset ISPE GAMP® 5 validation document templates and built in f...

Biology, chemistry and pharmacology data -all in one place. Accelerate drug development with early, comprehensive intelligence. Collating the necessary data to identify the likelihood of a drug's success as early as possible requires considerable resources. Cortellis Drug Discovery Intelligence(TM) ...

POWERFUL SERIALIZATION AND TRACEABILITY SOLUTION FOR L4-L5, NOW PART OF THE OPTCHAIN™ PLATFORM OPTEL’s L4-L5 serialization software, a powerful, enterprise-level serialization and traceability solution, has helped the world’s best-known brands protect their assets. Optchain Verify is an essential tool to ...

As a busy parent, managing a child's medication can be hard. Team Consulting integrated connectivity into a syringe to help parents keep track of their child’s medication through a smartphone app.

Using a small, low-cost sensor, this connected syringe automatically tracks when and how much drug...

Digitization solutions for preventive and predictive maintenance:

Rise to the challenges of digitalization with the new Rommelag Pharma Platform. This sophisticated solution honors the strict compliance stipulations of the pharmaceutical industry while leveraging automated techn...

Dec has developed an extensive range of isolator technologies which allow the flexible and safe handling of powders and a simple integration into multiple production processes.

Dec develops, designs and supplies turnkey process integrated containment technology solutions for both potent and asepti...

Our expertise lies in providing innovative solutions to drive digital transformation, fostering innovation and sustainable growth through strategic insight and collaborative partnerships.

SLIM was developed and validated to provide total management of your drug products placed on stability. SLIM has the rich feature set required to meet the challenges today’s Lab Supervisors and Stability Managers face on a daily basis. SLIM’s fast, intuitive user interface and exceptional reliability provi...

SoftGroup® SaTT EU Hub Gatewayoffers an upload/update of PMD (Product Master Data) and PPD (Product Pack Data) to the EU HUB (EMVO). Via this Cloud solution, the MAH / Parallel distributor could select which serialized batch should be reported to EMVO. The system allows status verification o...

Deliver your clinical breakthrough to market in record time. With kp’s next generation BlisterPro® services, you can gain a true competitive, cost-effective edge with turn-key blister package design, finite element analysis, tooling design, fabrication, and package production. As the leading pharmaceutical...

Increase successful submission outcomes in markets worldwide with comprehensive, expertly analyzed regulatory and market access information 1. Get treatments to patients faster Compare and monitor regulations quickly across markets to understand regional health technology assessment (HTA) outcomes. 2. Main...

SLIMStat is extremely easy-to-use software developed and validated specifically to determine the shelf life of drug products that have been placed on stability. This interactive and intuitive tool empowers non-statisticians the ability to generate statistical analyses with complete confidence. Fully v...

QEdge is an enterprise-wide Risk based, Quality management Software to ensure product Quality and regulatory compliance, and Audit Readiness.

·QEdge eQMS has configured 60 + Process

Data Integrity Part 11 (21 CFR Part 11, Annex 11) compliant Risk ...

We specialize in Computer System Validation, equipment validation, utility qualification, and IT and OT infrastructure qualification. Our services adhere to the regulatory standards of EMA, FDA, WHO, and other Life Science bodies in Europe and the Americas. With a track record of serving over 180 clients a...

Manufacturing Performance Monitoring Suit - A Prebuild, Plug & Play Solution that Fully addresses, all your KPIs to make Manufacturing Processes Lean, Shop Floor managers more Insightful, Efficient, Accountable and Connected with revenue in Real time. MPM will enlighten you with .
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Paperless Batch Manufacturing Record & Traceability Solution - Weighing + Recording + Tracking the batch from raw material to final packaging In Pharma. Planning dispensing facility, Raw material weighing, Dispensing based on Process order. Batching & Lot making in integration with ERP ...

Electronic fingerprint technology for product authentication.  450 ppm for carton authentication.  Smart phone authentication anywhere in the world. A new and simple way to ensure your products are tracked and uniquely identified  and that your end customers can check product authentici...

The Gruppo SASI’s solution, called PSMF Manager, for the management of the Pharmacovigilance System Master File, is developed in full compliance with the legislation in force for the European community published on the European Medicines Agency website (www.ema.europa.eu) whose legal requirement was i...

IntroductionGruppo SASI's offer for the management of the Technical File for Medical Devices is developed in full compliance with the legislation in force for the European community as illustrated in the REGULATION (EU) 2017/745 and 2017/746 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 5 April 201...